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The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Akt2 and SGK3 are both important for normal hair growth and development.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Keratin-gelatin films improve skin graft success in dogs.

Desmoglein 1 can partly make up for the loss of Desmoglein 3 in hair adhesion but not in mucous membranes.

The UHS promoter is specific to mouse hair follicles.

miR-140-y helps control feather growth in geese by affecting the Wnt signaling pathway.

The scraggly mutation causes hair loss and skin defects in mice.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

K6hf is a unique protein found only in a specific layer of hair follicles.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Combining FCS and MPG is more effective for treating stable vitiligo than using either alone.

Gefitinib treatment led to unexpected hair growth in two lung cancer patients.

Blocking hair follicle development stops key gene signals needed for hair growth in mice.

Isoginkgetin reduces inflammation in cells by blocking NF-κB activation.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

FGF and EGF are crucial for hair follicle development and growth.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

EGFR deficiency in skin causes hair follicle issues and inflammation.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

Fgfr2b helps maintain healthy skin and prevent cancer.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.